Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 986345Generated: October 25, 2026

Sodium hydride → isopropyl N-n-butoxymethyl-2-bromo-4-methyl-5-imidazolecarboxylate

https://huagongshe.com/reaction/986345

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant1-(Chloromethoxy)butaneHCID 11105357—
ReactantHCID 178432453HCID 178432453—
SolventTetrahydrofuranHCID 8028—
Productisopropyl N-n-butoxymethyl-2-bromo-4-methyl-5-imidazolecarboxylateHCID 1358903589%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of 293 milligrams (1.22 mM) of sodium hydride in 30 ml of anhydrous tetrahydrofuran was added, in portions, 3 g (1.22 mM) of isopropyl 2-bromo-4-methyl-5-imidazolecarboxylate. The resulting suspension was cooled to 0° C. and 1.5 g (1.22 mM) of chloromethyl-n-butyl ether was added dropwise. The reaction mixture was stirred overnight at room temperature. The precipitated sodium chloride was removed by filtration and concentration of the filtrate in vacuo gave 3.6 g of isopropyl N-n-butoxymethyl-2-bromo-4-methyl-5-imidazolecarboxylate as a golden oil (87%). Subsequent analysis indicated that the 3-isomer/1-isomer ratio was 91/9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04711962
Source datasetuspto-grants-1987_12
ORD IDord-89a68d88d12949dab80381831df1a89d
Source noteuspto-grants-1987_12